proline and Congenital Hypocupremia

proline has been researched along with Congenital Hypocupremia in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Mori, M; Nishimura, M	1

Other Studies

1 other study(ies) available for proline and Congenital Hypocupremia

Article	Year
A serine-to-proline mutation in the copper-transporting P-type ATPase gene of the macular mouse. Mammalian genome : official journal of the International Mammalian Genome Society, 1997, Volume: 8, Issue:6 Topics: Adenosine Triphosphatases; Animals; Carrier Proteins; Cation Transport Proteins; Copper-Transporting ATPases; Deoxyribonuclease BamHI; Disease Models, Animal; Female; Homozygote; Humans; Male; Menkes Kinky Hair Syndrome; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Point Mutation; Proline; Recombinant Fusion Proteins; Sequence Analysis, DNA; Serine	1997

Article

Year

A serine-to-proline mutation in the copper-transporting P-type ATPase gene of the macular mouse.

Mammalian genome : official journal of the International Mammalian Genome Society, 1997, Volume: 8, Issue:6

Topics: Adenosine Triphosphatases; Animals; Carrier Proteins; Cation Transport Proteins; Copper-Transporting ATPases; Deoxyribonuclease BamHI; Disease Models, Animal; Female; Homozygote; Humans; Male; Menkes Kinky Hair Syndrome; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Point Mutation; Proline; Recombinant Fusion Proteins; Sequence Analysis, DNA; Serine

1997